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HRID 1885759作成日:2026年10月27日

Ammonia → Muskone

https://huagongshe.com/reaction/1885759

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物TolueneHCID 1140—
反応物Ammonium ChlorideHCID 25517—
反応物2-CyclopentadecenoneHCID 54040345—
生成物MuskoneHCID 10947—

反応条件

温度-78 °C

反応手順

The solution was cooled to -78° C., and a solution of 0.3604 g (1.62 mmol) of 2-cyclopentadecenone in 1 ml of toluene was added thereto dropwise, followed by stirring at -78° C. for 17 hours. To the reaction mixture was added 4 ml of a 1:1 (by volume) mixture of aqueous ammonia and a saturated ammonium chloride aqueous solution, followed by heating up to room temperature. The aqueous layer was removed, and the organic layer was washed successively with a 1:1 (by volume) mixture of aqueous ammonia and a saturated ammonium chloride aqueous solution, a 5% hydrochloric acid aqueous solution, a saturated sodium chloride aqueous solution, and a saturated sodium carbonate aqueous solution, and dried over sodium sulfate. The toluene was removed by distillation, and the residue was purified by silica gel column chromatography using hexane/ethyl acetate (40:1 by volume) as an eluent and then distilled under reduced pressure to obtain an optically active muscone. The yield, optical rotation, optical purity, and stereochemistry of the product were determined, and the results obtained are shown in Table 1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05146003
出典データセットuspto-grants-1992_09
ORD IDord-981e45501dec4bb09b5131333c3d2662
出典メモuspto-grants-1992_09